# Amiodarone Hydrochloride

NDC: 62135-577
Generic name: Amiodarone Hydrochloride
Labeler / Manufacturer: Chartwell RX, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20130101

FDA application: ANDA077069

## Active ingredients

- AMIODARONE HYDROCHLORIDE: 200 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"62135-577"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=62135-577
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=5520f11d-968d-4f4f-bf57-d14369c0d746